Rifa S or Rifa S Sodium (Rifaint)
Rifamycin S or Rifamycin S sodium antibiotic substance
HSN 2941 90 13 (Rifa S or Rifa S Sodium) is subject to Narcotic Drugs and Psychotropic Substances (NDPS) import controls under Chapter VII-A of the NDPS Rules, 1985, with an import certificate required under Rule 53 of those Rules for medical and scientific purposes. Directorate General of Foreign Trade (DGFT) ITC (HS) policy condition 2 of Chapter 29 governs imports outside the medical and scientific category, and Central Board of Indirect Taxes and Customs (CBIC) Circular 23/2023-Cus dated 30-09-2023 mandates additional Chapter 29 qualifiers in the import declaration effective 15 October 2023.
- Import certificate from NDPS
- Import licence for drugs from CDSCO
- Registration certificate from CDSCO
Procedural directions for customs clearance are issued by: Directorate General of Foreign Trade, Central Board of Indirect Taxes and Customs.
- 1Obtain an import certificate under Rule 53 of the NDPS Rules, 1985 for medical or scientific use from the Central Bureau of Narcotics (details at http://cbn.nic.in). Upload the import licence for drugs (document code 9111dc) and the registration certificate for drugs (document code 101dc1) in e-Sanchit before filing the bill of entry.Chapter VII-A and Rule 53 of the NDPS Rules, 1985 · ITC (HS) policy condition 2 of Chapter 29
- 2Upload all mandatory e-Sanchit documents before out-of-charge: Certificate of Analysis — Drug (0010dc), Batch Release Certificate (0030dc), Label of Consignment (0110dc), Registration Certificate for Drugs (101dc1), and Import Licence for Drugs (9111dc). Customs proper officers verify these on PGA-facilitated bills where NOC routing has not occurred.CCR e-Sanchit mandatory document requirement · document codes 0010dc, 0030dc, 0110dc, 101dc1, 9111dc
- 3Include the mandatory additional qualifiers in the import declaration for Chapter 29 commodities as stipulated in paragraphs 4.1 and 4.2 of CBIC Circular 23/2023-Cus dated 30-09-2023. This requirement is operative with effect from 15 October 2023 and applies to all Chapter 29 entries.CBIC Circular 23/2023-Cus dated 30-09-2023, paragraphs 4.1 and 4.2
The most common error on this tariff line is failing to distinguish the two import tracks: imports for medical and scientific purposes require an NDPS import certificate under Rule 53, while all other imports are governed by Appendix-I of the ITC (HS) schedule under policy condition 2 of Chapter 29. Attempting to import under the medical and scientific track without a valid Rule 53 certificate — or misclassifying a commercial import as a medical-use consignment — attracts seizure and prosecution under the NDPS Act, 1985. Ensure the applicable track is established and documented before the bill of entry is filed.